Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population CM Hagen, FH Aidt, PL Hedley, MK Jensen, O Havndrup, JK Kanters, ... PloS one 8 (8), e71904, 2013 | 51 | 2013 |
Dysfunctional mitochondrial respiration in the striatum of the Huntington’s disease transgenic R6/2 mouse model FH Aidt, SMB Nielsen, J Kanters, D Pesta, TT Nielsen, A Nørremølle, ... PLoS currents 5, 2013 | 49 | 2013 |
The Role of CAV3 in Long–QT Syndrome: Clinical and Functional Assessment of a Caveolin-3/Kv11.1 Double Heterozygote Versus Caveolin-3 Single Heterozygote PL Hedley, JK Kanters, M Dembic, T Jespersen, L Skibsbye, FH Aidt, ... Circulation: Cardiovascular Genetics 6 (5), 452-461, 2013 | 38 | 2013 |
MT‐CYB mutations in hypertrophic cardiomyopathy CM Hagen, FH Aidt, O Havndrup, PL Hedley, C Jespersgaard, M Jensen, ... Molecular genetics & genomic medicine 1 (1), 54-65, 2013 | 35 | 2013 |
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2 M Christiansen, PL Hedley, J Theilade, B Stoevring, TP Leren, O Eschen, ... BMC medical genetics 15, 1-11, 2014 | 21 | 2014 |
SCA28: novel mutation in the AFG3L2 proteolytic domain causes a mild cerebellar syndrome with selective type-1 muscle fiber atrophy K Svenstrup, TT Nielsen, F Aidt, N Rostgaard, M Duno, F Wibrand, ... The Cerebellum 16, 62-67, 2017 | 19 | 2017 |
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy CM Hagen, FH Aidt, O Havndrup, PL Hedley, MK Jensen, JK Kanters, ... PLoS One 10 (4), e0124540, 2015 | 14 | 2015 |
Localization of A11‐reactive oligomeric species in prion diseases FH Aidt, LF Hasholt, M Christiansen, H Laursen Histopathology 62 (7), 994-1001, 2013 | 11 | 2013 |
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study PL Hedley, O Haundrup, PS Andersen, FH Aidt, M Jensen, ... Journal of Negative Results in BioMedicine 10, 1-5, 2011 | 11 | 2011 |
Dysfunctional mitochondrial respiration in the striatum of the Huntington’s disease transgenic R6/2 mouse model. PLoS Curr. 2013; 5 FH Aidt, SM Nielsen, J Kanters, D Pesta, TT Nielsen, A Norremolle, ... Epub 2013/04/10. https://doi. org/10.1371/currents. hd …, 0 | 4 | |
Evolutionary dissection of mtDNA hg H: A susceptibility factor for hypertrophic cardiomyopathy CM Hagen, JL Elson, PL Hedley, FH Aidt, O Havndrup, MK Jensen, ... Mitochondrial DNA Part A 31 (6), 238-244, 2020 | 3 | 2020 |
The role of CAV3 in long QT: clinical and functional assessment of a caveolin-3/Kc11. 1 compound heterozygote PL Hedley, JK Kanters, M Dembic, T Jesperson, L Skibsbye, FH Aidt, ... American Heart Association, 2013 | 3 | 2013 |
Erratum: MT-CYB mutations in hypertrophic cardiomyopathy CM Hagen, FH Aidt, O Havndrup, PL Hedley, C Jespersgaard, M Jensen, ... | | 2013 |